A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095085



Internal ID21283497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70144118..70368558hg38UCSC Ensembl
Innerchr14:70610835..70835275hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg38224441
hg19224441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113230
Supporting Variants
Samplessample345
Known GenesADAM21P1, COX16, SLC8A3, SYNJ2BP, SYNJ2BP-COX16
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095085
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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